M. Chang, M. Bellaoui, C. Zhang, R. Desai, and P. Morozov, RMI1/NCE4, a suppressor of genome instability, encodes a member of the RecQ helicase/Topo III complex, EMBO J, vol.24, pp.2024-2033, 2005.

T. M. Lohman, E. J. Tomko, and C. G. Wu, Nonhexameric DNA helicases and translocases: mechanisms and regulation, Nat Rev Mol Cell Biol, vol.9, pp.391-401, 2008.
DOI : 10.1038/nrm2394

L. Wu and I. D. Hickson, The Bloom's syndrome helicase suppresses crossing over during homologous recombination, Nature, vol.426, pp.870-874, 2003.
DOI : 10.1038/nature02253

A. R. Meetei, S. Sechi, M. Wallisch, D. Yang, and M. K. Young, A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome, Mol Cell Biol, vol.23, pp.3417-3426, 2003.
DOI : 10.1128/mcb.23.10.3417-3426.2003

URL : https://mcb.asm.org/content/23/10/3417.full.pdf

J. Yin, A. Sobeck, C. Xu, A. R. Meetei, and M. Hoatlin, BLAP75, an essential component of Bloom's syndrome protein complexes that maintain genome integrity, EMBO J, vol.24, pp.1465-1476, 2005.

J. R. Mullen, F. S. Nallaseth, Y. Q. Lan, C. E. Slagle, and S. J. Brill, Yeast Rmi1/Nce4 controls genome stability as a subunit of the Sgs1-Top3 complex, Mol Cell Biol, vol.25, pp.4476-4487, 2005.

T. R. Singh, A. M. Ali, V. Busygina, S. Raynard, and Q. Fan, BLAP18/RMI2, a novel OBfold-containing protein, is an essential component of the Bloom helicase-double Holliday junction dissolvasome, Genes Dev, vol.22, p.2856, 2008.

D. Xu, R. Guo, A. Sobeck, C. Z. Bachrati, and J. Yang, RMI, a new OB-fold complex essential for Bloom syndrome protein to maintain genome stability, Genes Dev, vol.22, p.2843, 2008.
DOI : 10.1101/gad.1708608

URL : http://genesdev.cshlp.org/content/22/20/2843.full.pdf

Y. Liu and S. C. West, More complexity to the Bloom's syndrome complex, Genes Dev, vol.22, pp.2737-2742, 2008.
DOI : 10.1101/gad.1732808

URL : http://genesdev.cshlp.org/content/22/20/2737.full.pdf

W. Bussen, S. Raynard, V. Busygina, A. K. Singh, and P. Sung, Holliday junction processing activity of the BLM-Topo IIIalpha-BLAP75 complex, J Biol Chem, vol.282, pp.31484-31492, 2007.

S. Raynard, W. Bussen, and P. Sung, A double Holliday junction dissolvasome comprising BLM, topoisomerase IIIalpha, and BLAP75, J Biol Chem, vol.281, pp.13861-13864, 2006.
DOI : 10.1074/jbc.c600051200

URL : http://www.jbc.org/content/281/20/13861.full.pdf

L. Wu, C. Z. Bachrati, J. Ou, C. Xu, and J. Yin, BLAP75/RMI1 promotes the BLM-dependent dissolution of homologous recombination intermediates, Proc Natl Acad Sci U S A, vol.103, pp.4068-4073, 2006.

C. Z. Bachrati, R. H. Borts, and I. D. Hickson, Mobile D-loops are a preferred substrate for the Bloom's syndrome helicase, Nucleic Acids Res, vol.34, pp.2269-2279, 2006.
DOI : 10.1093/nar/gkl258

URL : https://academic.oup.com/nar/article-pdf/34/8/2269/3708760/gkl258.pdf

D. V. Bugreev, X. Yu, E. H. Egelman, and A. V. Mazin, Novel pro-and anti-recombination activities of the Bloom's syndrome helicase, Genes Dev, vol.21, pp.3085-3094, 2007.
DOI : 10.1101/gad.1609007

URL : http://genesdev.cshlp.org/content/21/23/3085.full.pdf

H. W. Mankouri, H. P. Ngo, and I. D. Hickson, Shu proteins promote the formation of homologous recombination intermediates that are processed by Sgs1-Rmi1-Top3, Mol Biol Cell, vol.18, pp.4062-4073, 2007.

S. Gravel, J. R. Chapman, C. Magill, and S. P. Jackson, DNA helicases Sgs1 and BLM promote DNA double-strand break resection, Genes Dev, vol.22, pp.2767-2772, 2008.
DOI : 10.1101/gad.503108

URL : http://genesdev.cshlp.org/content/22/20/2767.full.pdf

M. B. Bagherieh-najjar, O. M. De-vries, J. Hille, and P. P. Dijkwel, Arabidopsis RecQI4A suppresses homologous recombination and modulates DNA damage responses, Plant J, vol.43, pp.789-798, 2005.
DOI : 10.1111/j.1365-313x.2005.02501.x

URL : https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1365-313X.2005.02501.x

F. Hartung, H. Plchová, and H. Puchta, Molecular characterisation of RecQ homologues in Arabidopsis thaliana, Nucleic Acids Res, vol.28, pp.4275-4282, 2000.
DOI : 10.1093/nar/28.21.4275

URL : https://academic.oup.com/nar/article-pdf/28/21/4275/9904816/284275.pdf

F. Hartung, S. Suer, and H. Puchta, Two closely related RecQ helicases have antagonistic roles in homologous recombination and DNA repair in Arabidopsis thaliana, Proc Natl Acad Sci U S A, vol.104, pp.18836-18841, 2007.

L. Chelysheva, D. Vezon, K. Belcram, G. Gendrot, and M. Grelon, The Arabidopsis BLAP75/ RMI1 homologue plys crucial roles in meiotic double strand break repair, PLoS Genet, vol.4, issue.12, 2008.

F. Hartung, S. Suer, A. Knoll, R. Wurz-wildersinn, and H. Puchta, , vol.3, p.1, 2008.

, Are Not Only Required for the Suppression of Somatic Crossovers but Are Also Essential for the Resolution of Meiotic Recombination Intermediates in Arabidopsis thaliana, PLoS Genet, vol.4, issue.12, p.1000285

T. Allers and M. Lichten, Differential timing and control of noncrossover and crossover recombination during meiosis, Cell, vol.106, pp.47-57, 2001.

L. E. Berchowitz and G. P. Copenhaver, Division of labor among meiotic genes, Nat Genet, vol.40, pp.266-267, 2008.

D. K. Bishop and D. Zickler, Early decision; meiotic crossover interference prior to stable strand exchange and synapsis, Cell, vol.117, pp.9-15, 2004.

G. V. Borner, N. Kleckner, and N. Hunter, Crossover/noncrossover differentiation, synaptonemal complex formation, and regulatory surveillance at the leptotene/zygotene transition of meiosis, Cell, vol.117, pp.29-45, 2004.

N. Hunter and N. Kleckner, The single-end invasion: an asymmetric intermediate at the double-strand break to double-holliday junction transition of meiotic recombination, Cell, vol.106, pp.59-70, 2001.

G. H. Jones and F. C. Franklin, Meiotic crossingover: obligation and interference, Cell, vol.126, pp.246-248, 2006.

C. Mezard, J. Vignard, J. Drouaud, and R. Mercier, The road to crossovers: plants have their say, Trends Genet, vol.23, pp.91-99, 2007.

L. Jessop and M. Lichten, Mus81/Mms4 endonuclease and Sgs1 helicase collaborate to ensure proper recombination intermediate metabolism during meiosis, Mol Cell, vol.31, pp.313-323, 2008.

S. D. Oh, J. P. Lao, A. F. Taylor, G. R. Smith, and N. Hunter, RecQ helicase, Sgs1, and XPF family endonuclease, Mus81-Mms4, resolve aberrant joint molecules during meiotic recombination, Mol Cell, vol.31, pp.324-336, 2008.

F. Couteau, F. Belzile, C. Horlow, O. Grandjean, and D. Vezon, Random chromosome segregation without meiotic arrest in both male and female meiocytes of a dmc1 mutant of Arabidopsis, Plant Cell, vol.11, pp.1623-1634, 1999.

J. Bleuyard, M. E. Gallego, and C. I. White, Meiotic defects in the Arabidopsis rad50 mutant point to conservation of the MRX complex function in early stages of meiotic recombination, Chromosoma, vol.113, pp.197-203, 2004.
URL : https://hal.archives-ouvertes.fr/inserm-00595811

W. Li, C. Chen, U. Markmann-mulisch, L. Timofejeva, and E. Schmelzer, The Arabidopsis AtRAD51 gene is dispensable for vegetative development but required for meiosis, Proc Natl Acad Sci U S A, vol.101, pp.10596-10601, 2004.

J. Higgins, J. Vignard, R. Mercier, A. G. Pugh, and F. C. Franklin, AtMSH5 partners AtMSH4 in the class I meiotic crossover pathway in Arabidopsis thaliana, but is not required for synapsis, Plant J, vol.55, pp.28-39, 2008.

X. Lu, X. Liu, L. An, W. Zhang, and J. Sun, The Arabidopsis MutS homolog AtMSH5 is required for normal meiosis, Cell Res, vol.18, pp.589-599, 2008.

R. Mercier, S. Jolivet, D. Vezon, E. Huppe, and L. Chelysheva, Two meiotic crossover classes cohabit in Arabidopsis: one is dependent on MER3,whereas the other one is not, Curr Biol, vol.15, pp.692-701, 2005.

S. Gangloff, B. De-massy, L. Arthur, R. Rothstein, and F. Fabre, The essential role of yeast topoisomerase III in meiosis depends on recombination, EMBO J, vol.18, pp.1701-1711, 1999.

P. M. Watt, E. J. Louis, R. H. Borts, and I. D. Hickson, Sgs1: a eukaryotic homologue of E. coli RecQ that interacts with topoisomerase II in vivo and is required for faithful chromosome segregation, Cell, vol.81, pp.253-260, 1995.

F. Hartung, S. Suer, T. Bergmann, and H. Puchta, The role of AtMUS81 in DNA repair and its genetic interaction with the helicase AtRecQ4A, Nucleic Acids Res, vol.34, pp.4438-4448, 2006.

G. Luo, I. M. Santoro, L. D. Mcdaniel, I. Nishijima, and M. Mills, Cancer predisposition caused by elevated mitotic recombination in Bloom mice, Nat Genet, vol.26, pp.424-429, 2000.

L. E. Berchowitz, K. E. Francis, A. L. Bey, and G. P. Copenhaver, The role of AtMUS81 in interference-insensitive crossovers in A. thaliana, PLoS Genet, vol.3, p.132, 2007.